An Optimal DF Based Method for Transient Stability Analysis

Abstract

The effect of energy on the natural environment has become increasingly severe as human consumption of fossil energy has increased. The capacity of the synchronous generators to keep working without losing synchronization when the system is exposed to severe faults such as short circuits is referred to as the power system's transient stability. As the power system's safe and stable operation and mechanism of action become more complicated, higher demands for accurate and rapid power system transient stability analysis are made. Current methods for analyzing transient stability are less accurate because they do not account for misclassification of unstable samples. As a result, this paper proposes a novel approach for analyzing transient stability. The key concept is to use deep forest (DF) and a neighborhood rough reduction approach together. Using the neighborhood rough sets, the original feature space is obtained by creating many optimal feature subsets at various granularity levels. Then, by deploying the DF cascade structure, the mapping connection between the transient stability state and the features is reinforced. The weighted voting technique is used in the learning process to increase the classification accuracy of unstable samples. When contrasted to current methods, simulation results indicate that the proposed approach outperforms them.

Synthetic Curcumin Analogues Present Antiflavivirus Activity In Vitro with Potential Multiflavivirus Activity from a Thiazolylhydrazone Moiety

“…Similarly, modifications of substituents over aromatic moieties in curcumin analogues could favour and enhance antiviral activity, as shown in the optimization of E protein inhibitors against DENV-2 [54]. Thiazolylhydrazone substituents have also shown other biological activities in the past, including antibacterial [64], antifungal [65], as well as anti-inflammatory [66] and antioxidant [67]. Additionally, the synthetic curcumin analogues with thiazolylhydrazone moieties proposed in this work could even be supported by the targets predicted from inhibitors' similarities, which were also available in different active compounds with designed thiazolylhydrazone moieties assessed by Jadav et al 2015 [54] against DENV-2.…”